Canonical Allele Identifier: CA2424680389
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795982C= , CM000685.2:g.37795982C= GRCh38
NC_000023.10:g.37655235C= , CM000685.1:g.37655235C= GRCh37
NC_000023.9:g.37540175C= NCBI36
NG_009065.1:g.20962C= , LRG_53:g.20962C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*24C= ENSP00000512461.1:n.*24C=
ENST00000696171.1:c.419C= ENSP00000512462.1:p.Thr140=
ENST00000696172.1:c.338-2973C= ENSP00000512463.1:n.338-2973C=
ENST00000378588.5:c.515C= MANE Select ENSP00000367851.4:p.Thr172=
ENST00000378588.4:c.515C= ENSP00000367851.4:p.Thr172=
ENST00000465127.1:c.171+369982C= ENSP00000417050.1:n.171+369982C=
NM_000397.3:c.515C= , LRG_53t1:c.515C= NP_000388.2:p.Thr172=
XM_011543890.1:c.209C= XP_011542192.1:p.Thr70=
NM_000397.4:c.515C= MANE Select NP_000388.2:p.Thr172=